RecallHawk

Summary

CPSC recall: Scuba Buoyancy Compensator Devices (BCDs) with LP inflator hose. By Cressi authorized dealers nationwide from March 2022 through August 2022 for between $250 and $1,200 for the fully assembled BCD.. Hazard: Defective metal fittings on the inflator hose can cause an airflow restriction and failure to inflate, or improper inflation of the BCD, posing a drowning hazard to the user.. Remedy: Consumers should immediately stop using the recalled scuba BCDs and contact Cressi-sub to receiv

Details

Source

CPSC Consumer Product Recall

External ID

9424

Action Date

2022-10-13

Status

Recalled

Category

consumer_product

Product Description

This recall involves Scuba Buoyancy Compensator Devices (BCDs) with LP inflator hoses. The LP inflator hoses attach to t

Context & Analysis

This is a unclassified recall.

This was one of 13 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Frequently Asked Questions

What is a FDA recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Cressi authorized dealers nationwide from March 2022 through August 2022 for between $250 and $1,200 for the fully assembled BCD.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Cressi authorized dealers nationwide from March 2022 through August 2022 for between $250 and $1,200 for the fully assembled BCD. have FDA actions?

This is the only FDA action we have on record for Cressi authorized dealers nationwide from March 2022 through August 2022 for between $250 and $1,200 for the fully assembled BCD. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "9424" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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